Okada Haruhiko, Kimura Makoto T, Tan Dongfeng, Fujiwara Kyoko, Igarashi Jun, Makuuchi Masatoshi, Hui Ai-Min, Tsurumaru Masahiko, Nagase Hiroki
Department of Cancer Genetics, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.
Int J Oncol. 2005 Feb;26(2):369-77.
Expression profiling analysis revealed ectopic high expression of mouse TFF3 in non-tumor liver tissues from the hepatocellular carcinoma (HCC) susceptible PWK/Rbrc strain. TFF3 is a member of the trefoil factor family peptides, which are small secreted proteins regulating mucosal regeneration and repair, and which are overexpressed during inflammatory processes and cancer progression. We, therefore, analyzed the TFF3 expression extensively in mouse and human HCCs. Expression of the mouse TFF3 gene was significantly increased in 6 out of 7 HCCs from a PWK spontaneous tumor model and in all 7 HCCs from an SV40T antigen-induced transgenic MT-D2C57BL/6 model. In humans, 8 of 20 HCCs (40%) had overexpression of TFF3 in both mRNA level and protein level. We then analyzed DNA methylation patterns of the TFF3 promoter region to evaluate expression regulation of promoter methylation. In mouse HCCs, we demonstrated that two CpGs, at positions -992 and +109, were hypomethylated in 13 of 14 mouse HCCs. In human HCCs, hypomethylation at CpG -260 was associated with TFF3 overexpression (p=0.04). These results indicate that TFF3 overexpression may be a critical process in mouse and human hepatocellular carcinogenesis, and the specific promoter CpG hypomethylation may be one of the regulation mechanisms of TFF3 overexpression in HCCs.
表达谱分析显示,在肝细胞癌(HCC)易感PWK/Rbrc品系的非肿瘤肝组织中,小鼠TFF3异位高表达。TFF3是三叶因子家族肽的成员之一,三叶因子家族肽是一类小的分泌蛋白,可调节黏膜再生和修复,在炎症过程和癌症进展期间过表达。因此,我们广泛分析了小鼠和人类肝癌中TFF3的表达情况。在PWK自发肿瘤模型的7个肝癌中有6个以及在SV40T抗原诱导的转基因MT-D2C57BL/6模型的所有7个肝癌中,小鼠TFF3基因的表达均显著增加。在人类中,20个肝癌中有8个(40%)在mRNA水平和蛋白质水平均有TFF3过表达。然后,我们分析了TFF3启动子区域的DNA甲基化模式,以评估启动子甲基化的表达调控。在小鼠肝癌中,我们发现14个小鼠肝癌中有13个在-992和+109位置的两个CpG位点发生了低甲基化。在人类肝癌中,CpG -260位点的低甲基化与TFF3过表达相关(p=0.04)。这些结果表明,TFF3过表达可能是小鼠和人类肝细胞癌发生过程中的一个关键过程,特定启动子CpG位点的低甲基化可能是肝癌中TFF3过表达的调控机制之一。